Multifunctional bilayer scaffold for dental pulp protection and sustained calcium hydroxide release for mineralized tissue regeneration

Injury to the mineralized tissues that protect the dental pulp can lead to pulp exposure and inflammation, necessitating the use of biologically active materials capable of preserving pulp vitality. While current biomaterials such as mineral trioxide aggregate (MTA) are widely used in vital pulp therapy (VPT), their high cost, challenging handling, and lack of structural flexibility highlight the need for alternatives. Here, we introduce a multifunctional bilayer scaffold composed of a polycaprolactone (PCL) film and a PCL/poly(ethylene oxide) (PCL/PEO) blend loaded with calcium hydroxide (CH), designed to provide both cytoprotection and mineralized tissue regeneration. The scaffold features a compact PCL layer, acting as a barrier to protect the pulp from external cytotoxic agents, and a CH-loaded fibrillar PCL/PEO electrospun layer, aimed at promoting odontoblastic differentiation through sustained calcium ion release. The bilayer structure demonstrated mechanical stability and a degradation profile suitable for clinical application. The release mechanism relies on gradual fiber degradation and CH dissolution. In vitro, the fibrillar layer enhanced calcium ion release, supported dental pulp stem cell adhesion and viability, and stimulated mineralized matrix formation. The compact layer preserved cell viability even in the presence of glass ionomer cement. In vivo, the bilayer scaffold elicited a comparable inflammatory response and expression of dentinogenesis and angiogenesis markers relative to MTA, although it did not attain the same level of mineralized tissue formation. Overall, our results indicate that this multifunctional bilayer scaffold offers a cost-effective, dual-purpose alternative to current materials, with potential for further optimization of its tissue regeneration capabilities prior to clinical implementation.

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Publication Details

Journal
Biomaterials
Published
2025-09-16
DOI
https://doi.org/10.1016/j.biomaterials.2025.123700
Citations
2
Primary Topic
Bone Tissue Engineering Materials
Type
article
Field-Weighted Citation Impact
1.35
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article

Multifunctional bilayer scaffold for dental pulp protection and sustained calcium hydroxide release for mineralized tissue regeneration

Renan Dal‐Fabbro, Shun Min Chang, Alexandre Henrique dos Reis‐Prado, Igor Paulino Mendes Soares et al.
2 citations
Biomaterials
Bone Tissue Engineering Materials
1.35
article

Multifunctional bilayer scaffold for dental pulp protection and sustained calcium hydroxide release for mineralized tissue regeneration

Renan Dal‐Fabbro, Shun Min Chang, Alexandre Henrique dos Reis‐Prado, Igor Paulino Mendes Soares, Carlos Alberto de Souza Costa, Ana Beatriz Gomes de Carvalho, Marco C. Bottino, Josimeri Hebling, Caroline Anselmi, Pedro Oliveira
article en
2 citations

Abstract

Injury to the mineralized tissues that protect the dental pulp can lead to pulp exposure and inflammation, necessitating the use of biologically active materials capable of preserving pulp vitality. While current biomaterials such as mineral trioxide aggregate (MTA) are widely used in vital pulp therapy (VPT), their high cost, challenging handling, and lack of structural flexibility highlight the need for alternatives. Here, we introduce a multifunctional bilayer scaffold composed of a polycaprolactone (PCL) film and a PCL/poly(ethylene oxide) (PCL/PEO) blend loaded with calcium hydroxide (CH), designed to provide both cytoprotection and mineralized tissue regeneration. The scaffold features a compact PCL layer, acting as a barrier to protect the pulp from external cytotoxic agents, and a CH-loaded fibrillar PCL/PEO electrospun layer, aimed at promoting odontoblastic differentiation through sustained calcium ion release. The bilayer structure demonstrated mechanical stability and a degradation profile suitable for clinical application. The release mechanism relies on gradual fiber degradation and CH dissolution. In vitro, the fibrillar layer enhanced calcium ion release, supported dental pulp stem cell adhesion and viability, and stimulated mineralized matrix formation. The compact layer preserved cell viability even in the presence of glass ionomer cement. In vivo, the bilayer scaffold elicited a comparable inflammatory response and expression of dentinogenesis and angiogenesis markers relative to MTA, although it did not attain the same level of mineralized tissue formation. Overall, our results indicate that this multifunctional bilayer scaffold offers a cost-effective, dual-purpose alternative to current materials, with potential for further optimization of its tissue regeneration capabilities prior to clinical implementation.

BiomaterialsVol. 326
Universidade Federal de Minas Gerais (BR), University of Michigan (US), Michigan Medicine (US), Centro Universitário de Araraquara (BR), Universidade Estadual Paulista (Unesp) (BR)
Openalex Percentile: Top 17%
Bone Tissue Engineering Materials
1.35
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